Canonical Allele Identifier: CA2319221823

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094709_4094710delinsAC , CM000681.2:g.4094709_4094710delinsAC	GRCh38
NC_000019.9:g.4094707_4094708delinsAC , CM000681.1:g.4094707_4094708delinsAC	GRCh37
NC_000019.8:g.4045707_4045708delinsAC	NCBI36
NG_007996.1:g.34419_34420delinsGT , LRG_750:g.34419_34420delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-212_1486-211delinsGT
ENST00000688002.1:n.3198-212_3198-211delinsGT
ENST00000688751.1:n.183-212_183-211delinsGT
ENST00000689792.1:n.951-212_951-211delinsGT
ENST00000262948.10:c.1047-212_1047-211delinsGT MANE Select	ENSP00000262948.4:n.1047-212_1047-211delinsGT
ENST00000262948.9:c.1047-212_1047-211delinsGT	ENSP00000262948.3:n.1047-212_1047-211delinsGT
ENST00000394867.8:c.756-212_756-211delinsGT	ENSP00000378336.1:n.756-212_756-211delinsGT
ENST00000597263.5:n.232-212_232-211delinsGT
ENST00000599021.1:c.157-212_157-211delinsGT
ENST00000600584.5:n.2284_2285delinsGT
ENST00000601786.5:n.1348-212_1348-211delinsGT
NM_030662.3:c.1047-212_1047-211delinsGT , LRG_750t1:c.1047-212_1047-211delinsGT	NP_109587.1:n.1047-212_1047-211delinsGT
XM_006722799.2:c.768-212_768-211delinsGT	XP_006722862.1:n.768-212_768-211delinsGT
XM_011528133.1:c.477-212_477-211delinsGT	XP_011526435.1:n.477-212_477-211delinsGT
XM_017026989.1:c.1383_1384delinsGT	XP_016882478.1:p.Gly461=
XM_017026990.1:c.1104_1105delinsGT	XP_016882479.1:p.Gly368=
NM_030662.4:c.1047-212_1047-211delinsGT MANE Select	NP_109587.1:n.1047-212_1047-211delinsGT